A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610595



Internal ID16398004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:16116761..16158503hg38UCSC Ensembl
Innerchr8:15974270..16016012hg19UCSC Ensembl
Innerchr8:16018641..16060383hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3841743
hg1941743
hg1841743
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12024n54
Supporting Variantsnssv1106988
Samples
Known GenesMSR1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610595
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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